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Dimethyl Sulfoxide → HCID 22923382、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethyl Sulfoxide | HCID 679 | — |
| 反応物 | 4-Methanesulfonyl-6,7-dimethoxy-1,2,3-benzotriazine | HCID 14713860 | — |
| 反応物 | 1,2,3,4-Tetrahydro-1,6-dimethyl-2,4-dioxo-3-(4-piperidinyl)quinazoline hydrobromide | HCID 21851222 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | HCID 22923382 | HCID 22923382 | 67% |
反応手順
The procedure similar to that described in Example 40 was repeated, except that 354.0 mg (1.0 mmol) of 1,2,3,4-tetrahydro-1,6-dimethyl-2,4-dioxo-3-(4-piperidinyl)-quinazoline hydrobromide (Compound v) obtained in Example 41 was used, 4-methanesulfonyl-6,7-dimethoxy-1,2,3-benzotriazine was used in place of 4-chloro-6,7-dimethoxyquinazoline, DMSO was used as a reaction solvent in place of methanol, and the reaction was conducted at room temperature. As a result, 307.6 mg (yield: 67%) of Compound 75 was obtained as white crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05624926 |
| 出典データセット | uspto-grants-1997_04 |
| ORD ID | ord-25b78c8889bb41eb925ff373b6b6f769 |
| 出典メモ | uspto-grants-1997_04 |